Canonical Allele Identifier: CA127233173

Gene: RAD50 TH2LCRR

Linked Data

• dbSNP Id: rs565672160
• gnomAD v3: 5-132635256-G-A
• gnomAD v4: 5-132635256-G-A
• MyVariant Identifiers: chr5:g.131970948G>A (hg19) ; chr5:g.132635256G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132635256G>A , CM000667.2:g.132635256G>A	GRCh38
NC_000005.9:g.131970948G>A , CM000667.1:g.131970948G>A	GRCh37
NC_000005.8:g.131998847G>A	NCBI36
NG_021151.1:g.83333G>A
NG_021151.2:g.83280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3390-1859G>A (RAD50) MANE Select	ENSP00000368100.4:n.3390-1859G>A
ENST00000638452.2:c.3093-1859G>A	ENSP00000492349.2:n.3093-1859G>A
ENST00000638504.1:n.2998-1859G>A
ENST00000638568.2:c.3093-1859G>A	ENSP00000491158.2:n.3093-1859G>A
ENST00000639899.1:n.3909-1859G>A
ENST00000640655.2:c.3093-1859G>A	ENSP00000491596.2:n.3093-1859G>A
ENST00000651249.1:c.226-1859G>A (RAD50)
ENST00000378823.7:c.3390-1859G>A (RAD50)	ENSP00000368100.4:n.3390-1859G>A
ENST00000455677.1:c.25-1859G>A (RAD50)
ENST00000533482.5:c.*3016-1859G>A (RAD50)	ENSP00000431225.1:n.*3016-1859G>A
NM_005732.3:c.3390-1859G>A (RAD50)	NP_005723.2:n.3390-1859G>A
NR_132124.1:n.153+2902C>T (TH2LCRR)
NM_005732.4:c.3390-1859G>A (RAD50) MANE Select	NP_005723.2:n.3390-1859G>A